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Ultramicroscopy: development and outlook.
Dodt, Hans-Ulrich; Saghafi, Saiedeh; Becker, Klaus; Jährling, Nina; Hahn, Christian; Pende, Marko; Wanis, Martina; Niendorf, Axel.
Afiliación
  • Dodt HU; Vienna University of Technology, FKE, Chair of Bioelectronics, Floragasse 7, 1040 Vienna, Austria; Medical University of Vienna, Center for Brain Research, Spitalgasse 4, 1090 Vienna, Austria.
  • Saghafi S; Vienna University of Technology, FKE, Chair of Bioelectronics, Floragasse 7, 1040 Vienna, Austria; Medical University of Vienna, Center for Brain Research, Spitalgasse 4, 1090 Vienna, Austria.
  • Becker K; Vienna University of Technology, FKE, Chair of Bioelectronics, Floragasse 7, 1040 Vienna, Austria; Medical University of Vienna, Center for Brain Research, Spitalgasse 4, 1090 Vienna, Austria.
  • Jährling N; Vienna University of Technology, FKE, Chair of Bioelectronics, Floragasse 7, 1040 Vienna, Austria; Medical University of Vienna, Center for Brain Research, Spitalgasse 4, 1090 Vienna, Austria.
  • Hahn C; Vienna University of Technology, FKE, Chair of Bioelectronics, Floragasse 7, 1040 Vienna, Austria; Medical University of Vienna, Center for Brain Research, Spitalgasse 4, 1090 Vienna, Austria.
  • Pende M; Vienna University of Technology, FKE, Chair of Bioelectronics, Floragasse 7, 1040 Vienna, Austria; Medical University of Vienna, Center for Brain Research, Spitalgasse 4, 1090 Vienna, Austria.
  • Wanis M; Vienna University of Technology, FKE, Chair of Bioelectronics, Floragasse 7, 1040 Vienna, Austria; Medical University of Vienna, Center for Brain Research, Spitalgasse 4, 1090 Vienna, Austria.
  • Niendorf A; Pathologie Hamburg-West , Lornsenstraße 4, 22767 Hamburg, Germany.
Neurophotonics ; 2(4): 041407, 2015 Oct.
Article en En | MEDLINE | ID: mdl-26730396
ABSTRACT
We present an overview of the ultramicroscopy technique we developed. Starting from developments 100 years ago, we designed a light sheet microscope and a chemical clearing to image complete mouse brains. Fluorescence of green fluorescent protein (GFP)-labeled neurons in mouse brains could be preserved with our 3DISCO clearing and high-resolution three-dimensional (3-D) recordings were obtained. Ultramicroscopy was also used to image whole mouse embryos and flies. We improved the optical sectioning of our light sheet microscope by generating longer and thinner light sheets with aspheric optics. To obtain high-resolution images, we corrected available air microscope objectives for clearing solutions with high refractive index. We discuss how eventually super resolution could be realized in light sheet microscopy by applying stimulated emission depletion technology. Also the imaging of brain function by recording of mouse brains expressing cfos-GFP is discussed. Finally, we show the first 3-D recordings of human breast cancer with light sheet microscopy as application in medical diagnostics.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Neurophotonics Año: 2015 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Neurophotonics Año: 2015 Tipo del documento: Article País de afiliación: Austria
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